Wong Shannon, Nagengast Eric S, Miller Jason
*Division of Plastic and Reconstructive Surgery, University of Nebraska Medical Center†University of Nebraska College of Medicine, Omaha, NE.
J Craniofac Surg. 2016 May;27(3):e283-8. doi: 10.1097/SCS.0000000000002452.
Normocephalic pancraniosynostosis is a rare form of craniosynostosis that usually presents later in life secondary to a delayed onset of symptoms and the presence of a normal head shape. Since its initial description in the literature in 2010, normocephalic pancraniosynostosis remains a rare clinical entity that has only been reported in 6 patients. Surgical treatment in the 2 published reports has been by staged total calvarial reconstruction or anterior cranial vault remodeling with bilateral frontoorbital advancement. In this case report, the authors present 1 patient with normocephalic pancraniosynostosis and propose surgical treatment by anterior cranial vault expansion with distraction osteogenesis.
正常头颅型全颅缝早闭是一种罕见的颅缝早闭形式,通常在生命后期出现,原因是症状出现延迟且头部形状正常。自2010年在文献中首次描述以来,正常头颅型全颅缝早闭仍然是一种罕见的临床实体,仅在6例患者中报道过。在2篇已发表的报告中,手术治疗采用分期全颅骨重建或双侧额眶前移的前颅 vault 重塑。在本病例报告中,作者介绍了1例正常头颅型全颅缝早闭患者,并提出通过牵张成骨进行前颅 vault 扩张的手术治疗方法。